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ICARUS-LUNG01 dataset
Dataset
EGAD50000001014
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Whole genome sequencing data of paediatric hyperdiploid acute lymphoblastic leukemia
Study
EGAS50000001690
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The landscape of somatic mutations in epigenetic regulators across 1000 pediatric cancer genomes
Study
EGAS00001000449
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Single-cell transcriptome analysis of B-cell development in the ABO platform
Dataset
EGAD50000002433
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Personalized IGM, IGK, IGL V(D)J repertoire sequencing of four Influenza A exposed individuals
Dataset
EGAD50000002018
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UCSF WCDT WGS/WGBS mCRPC
Study
EGAS00001006649
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HipSci___Whole_Exome_sequencing___Congenital_hyperinsulinia
Study
EGAS00001001977
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HipSci___Whole_Exome_sequencing___Kabuki
Study
EGAS00001001981
-
HipSci HumanExome BeadChip analysis - Hereditary Cerebellar Ataxias
Study
EGAS00001002005
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The genomic landscape of Burkitt Lymphoma
Study
EGAS00001002198
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POT1_splice_site_mutant_analysis
Study
EGAS00001000571
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Personalized RNA mutanome vaccines mobilize poly-specific therapeutic immunity against cancer
Study
EGAS00001003306
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Identification of Long Non-coding RNA Biomarker of Human Lupus Nephritis Disease Activity
Study
EGAS00001007117
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Whole-exome sequencing performed on a patient with chronic myelomonocytic leukemia and B cell acute lymphoblastic leukemia
Study
EGAS00001005117
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CMML Collection of WES, WGS, RNA-Seq and ERRBS data
Study
EGAS00001001264
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HipSci HumanExome BeadChip analysis - monogenic diabetes
Study
EGAS00001001273
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HipSci___Whole_Exome_sequencing___Cardiomyopathy
Study
EGAS00001001980
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HipSci HumanExome BeadChip analysis - Kabuki syndrome
Study
EGAS00001002007
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HipSci HumanExome BeadChip analysis - Macular Dystrophy
Study
EGAS00001002014
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The_Little_Princess_Knowledge_Bank_RNAseq
Study
EGAS00001005244
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HipSci___Whole_Exome_sequencing___Alport
Study
EGAS00001001974
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HipSci HumanHT 12 Expression BeadChip analysis - Retinitis Pigmentosa
Study
EGAS00001002030
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Familial_Thrombocytosis_germline_exome_sequencing
Study
EGAS00001000088
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Mixed_Leukemia_Rearrangement_Screen
Study
EGAS00001000180
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Genetic_screening__of_GPI_anchor_protein_synthesis__
Study
EGAS00001001256
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Whole genome landscape of 25 metastatic cutaneous squamous cell carcinoma cSCC patients
Study
EGAS00001006378
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HipSci___Whole_Exome_sequencing___Retinitis_Pigmentosa
Study
EGAS00001001984
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Diverse modes of genomic alterations in hepatocellular carcinoma
Study
EGAS00001000824
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Imaging metabolic heterogeneity in breast cancer using hyperpolarized 13C-MRI
Study
EGAS00001004118
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16S rRNA gene amplification and maternal factors
Study
EGAS00001003044
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ARGO_GWAS
Study
EGAS00001000917
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Myelodysplastic_Syndrome_Exome_Sequnecing
Study
EGAS00001000089
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HipSci Illumina 450K Methylation analysis-Rare_BBS
Study
EGAS00001001274
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Whole_Genome_sequencing_of_individuals_from_Carlantino__Italy
Study
EGAS00001000460
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Congenital_anosmia_2
Study
EGAS00001001429
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Genomic and transcriptomic profiling of signalling networks in follicular lymphoma
Study
EGAS00001002175
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Developing somatic copy number and mutation calling tools for a bespoke sequencing platform
Study
EGAS00001007195
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Analysis of Loose Ends in Cancer Genome Structure
Study
EGAS00001007324
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B Cell Receptor Study From Metastatic Breast Cancer Tumour Samples
Study
EGAS00001006976
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HipSci___Whole_Exome_sequencing___Bardet_Biedl_Syndrome
Study
EGAS00001000969
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HipSci___Whole_Exome_sequencing___BPD
Study
EGAS00001001976
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HipSci___Whole_Exome_sequencing___Ataxia
Study
EGAS00001001978
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HipSci HumanExome BeadChip analysis - Alport Syndrome
Study
EGAS00001002009
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HipSci HumanExome BeadChip analysis - Retinitis Pigmentosa
Study
EGAS00001002015
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HipSci HumanHT 12 Expression BeadChip analysis - Kabuki syndrome
Study
EGAS00001002022
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HipSci HumanHT 12 Expression BeadChip analysis - Congenital Hyperinsulinia
Study
EGAS00001002025
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HipSci Illumina 450K Methylation analysis - monogenic diabetes
Study
EGAS00001001275
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Inherited genetic predisposition to childhood acute lymphoblastic leukemia investigated using a genome wide association study.
Study
EGAS00001002809
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HipSci___Whole_Exome_sequencing___Monogenic_Diabetes
Study
EGAS00001001140
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Transcriptomes_of_human_lymphocytes
Study
EGAS00001001755
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APCDR AGV Project: WGS of South African Zulu
Study
EGAS00001000286
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Determination of the molecular nature of the Vel blood group by exome sequencing
Study
EGAS00001000069
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HipSci genotyping microarray for embryonic stem cell control lines
Study
EGAS00001001730
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Whole-exome sequencing of PTC, benign nodule and normal tissues in 28 patients
Study
EGAS00001002312
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Subclonal evolution of four ER+ breast cancers determined by WGS and scRNA-Seq
Study
EGAS00001002436
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Total RNAseq in the sporadic ALS and healthy control motor cortex
Study
EGAS00001004286
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ET_Exome
Study
EGAS00001000102
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We performed whole-exome sequencing and whole epigenome sequencing (RRBS) of samples collected from different time points during radiotherapy from thirty-four ESCC patients. We compared the genetic and epigenetic features of the different time biopsy samples to reveal the changes in ESCC received radiotherapy.
Study
EGAS00001002719
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De_novo_mutations_in_cell_free_foetal_DNA__cffDNA_
Study
EGAS00001000322
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Ancient nuclear genomes enable repatriation of Indigenous human remains
Study
EGAS00001003359
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Glioma_cell_lines_rearrangement_screen
Study
EGAS00001000202
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Capture Hi-C on Hodgkin lymphoma cell line L-428
Study
EGAS00001003032
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HipSci Methylation analysis for embryonic stem cell control lines
Study
EGAS00001001728
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Renal_Follow_Up_Series
Study
EGAS00001000095
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Personalized RNA mutanome vaccines mobilize poly-specific therapeutic immunity against cancer RNA-Seq
Study
EGAS00001003307
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APCDR AGV Project: WGS of an Ugandan population
Study
EGAS00001000363
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Molecular profiling of DLBCL patients treated in the HOVON84 trial
Study
EGAS00001003949
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HipSci HumanExome BeadChip analysis-Healthy volunteers
Study
EGAS00001000866
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Whole-exome sequencing of extranodal NK/T cell lymphoma
Study
EGAS00001004357
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Skeletal muscle transcriptomic comparison between long-term trained and untrained men and women
Study
EGAS00001004367
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HipSci HumanExome BeadChip analysis-Rare_BBS
Study
EGAS00001001272
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Amplicon_based_sequencing_of_drug_resistant_lung_cancer_cell_lines
Study
EGAS00001001675
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The evolution of adult T-cell acute lymphoblastic leukemia
Study
EGAS00001004750
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Exome_Sequencing_of_Poor_Prognosis_Acute_Myeloid_Leukaemia
Study
EGAS00001000146
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HipSci___Whole_Exome_sequencing___HSP
Study
EGAS00001001979
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Non_Tumour_Renal_Cell_Line_Sequencing
Study
EGAS00001000205
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HipSci HumanExome BeadChip analysis - Primary immune deficiency
Study
EGAS00001002012
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Test_of_PCR_library_method_on_whole_genmoe_samples
Study
EGAS00001000214
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Genome_Diversity_in_Africa_Project___GemCode_libraries_
Study
EGAS00001001828
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Illumina HiSeqX whole genome sequence data on 58 samples including 54 with known HTT triplet repeat expansions (2 premutation and 52 full expansions)
Study
EGAS00001002593
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Analysis of transcriptomic profiles from affected and recovered muscle biopsies from children with reversible infantile respiratory chain deficiency.
Study
EGAS00001004647
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Whole transcriptome and exome sequencing of childhood ALL
Study
EGAS00001001858
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Normal brain controls for ICGC PedBrain DNA methylation sequencing
Study
EGAS00001000909
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Proteotranscriptomic classification and characterization of pancreatic neuroendocrine neoplasms
Study
EGAS00001005024
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HipSci___Whole_Exome_sequencing___Battens
Study
EGAS00001001975
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Mapping_genetic_variants_underlying_gene_regulation_in_inflammed_intestinal_cell_types_to_identify_novel_IBD_drug_targets
Study
EGAS00001003770
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HipSci___Whole_Exome_sequencing___Macular_dystrophy
Study
EGAS00001001982
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HipSci___Whole_Exome_sequencing___PID
Study
EGAS00001001983
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HipSci HumanExome BeadChip analysis - Hereditary Spastic Paraplegia
Study
EGAS00001002006
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HipSci HumanExome BeadChip analysis - Congenital Hyperinsulinia
Study
EGAS00001002010
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HipSci HumanExome BeadChip analysis - Hypertrophic Cardiomyopathy
Study
EGAS00001002011
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HipSci HumanExome BeadChip analysis - Battens disease
Study
EGAS00001002016
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HipSci HumanHT 12 Expression BeadChip analysis - Alport syndrome
Study
EGAS00001002024
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HipSci HumanHT 12 Expression BeadChip analysis - Hypertrophic Cardiomyopathy
Study
EGAS00001002026
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HipSci HumanHT 12 Expression BeadChip analysis - Macular Dystrophy
Study
EGAS00001002029
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HipSci HumanHT 12 Expression BeadChip analysis - Battens disease
Study
EGAS00001002031
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Whole-genome bisulfite sequencing analysis of low-grade astrocytomas in the ICGC PedBrain Tumor Project
Study
EGAS00001004019
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Transcriptomic and epigentic analysis of human peripheral blood NK cell subsets revealing role of Bcl11b in differentiation
Study
EGAS00001005025
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Brain transcriptome of hereditary cerebral haemorrhage with amyloidosis–Dutch type (HCHWA-D)
Study
EGAS00001002730
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INSIGHT: VHL Case Report
Study
EGAS00001005895